From Wikipedia, the free encyclopedia
Pirenzepine (Gastrozepin ), an M1 selective antagonist, is used in the treatment of peptic ulcers , as it reduces gastric acid secretion and reduces muscle spasm . It is in a class of drugs known as muscarinic receptor antagonists - acetylcholine being the neurotransmitter of the parasympathetic nervous system which initiates the rest-and-digest state (as opposed to fight-or-flight), resulting in an increase in gastric motility and digestion; whereas pirenzepine would inhibit these actions and cause decreased gastric motility leading to delayed gastric emptying and constipation.[ 1] It has no effects on the brain and spinal cord as it cannot diffuse through the blood–brain barrier .
Pirenzepine has been investigated for use in myopia control.[ 2] [ 3]
It promotes the homodimerization or oligomerisation of M1 receptors .[ 4]
See also
References
^ Stolerman IP (2 August 2010). Encyclopedia of Psychopharmacology . Springer. p. 811. ISBN 978-3-540-68698-9 . Retrieved 26 June 2013 .
^ Czepita D (2005). "[Fundamentals of modern treatment of myopia]". Annales Academiae Medicae Stetinensis . 51 (2): 5–9. PMID 16519089 .
^ Walline, Jeffrey J.; Lindsley, Kristina B.; Vedula, S. Swaroop; Cotter, Susan A.; Mutti, Donald O.; Ng, Sueko M.; Twelker, J. Daniel (13 January 2020). "Interventions to slow progression of myopia in children" . The Cochrane Database of Systematic Reviews . 1 : CD004916. doi :10.1002/14651858.CD004916.pub4 . ISSN 1469-493X . PMC 6984636 . PMID 31930781 .
^ Pediani JD, Ward RJ, Godin AG, Marsango S, Milligan G (June 2016). "Dynamic Regulation of Quaternary Organization of the M1 Muscarinic Receptor by Subtype-selective Antagonist Drugs" . The Journal of Biological Chemistry . 291 (25): 13132–46. doi :10.1074/jbc.M115.712562 . PMC 4933229 . PMID 27080256 . {{cite journal }}
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